Clinical Trial Management & Monitoring

A critical factor in our commitment to quality is the consistency we provide our clients. Many of our Project Managers have worked with clients on multiple studies. They have an excellent understanding of how to meet the specific needs of different clients.

At CTMS, we get to know our clients. This knowledge is what allows us to consistently exceed their expectations, and that’s what keeps them coming back.

With each clinical trial, the CTMS team participates in protocol specific training to ensure that all team members fully understand the protocol and their responsibilities.

We offer a full array of services.

Project management
Investigative site management and monitoring
Investigator identification and recruitment
Study related binders/document preparation
Clinical supplies and CRF storage and shipment
Investigator agreement and grant payment management
IRB management
Central laboratory management
Regulatory document/consent form approval and submission
AE/SAE reporting
Medical monitoring
CRF tracking
Study file management

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